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Review
. 2002 Mar 5;166(5):616-23.

Advances in the pharmacotherapy of Alzheimer's disease

Affiliations
Review

Advances in the pharmacotherapy of Alzheimer's disease

Serge Gauthier. CMAJ. .
No abstract available

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Figures

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Fig. 1: Synthesis of the neurotransmitter acetylcholine (ACh) from acetyl coenzyme A (AcCoA) and choline through the action of the enzyme choline acetyltransferase (ChAT). Acetylcholine is released into the synaptic cleft and acts on multiple sites including presynaptic nicotinic (N) and muscarinic type 2 (M2) receptors — exerting positive (+) and negative (–) action on further release of acetylcholine — and postsynaptic muscarinic type 1 (M1) receptors. Acetylcholinesterase (AChE) breaks acetylcholine down into choline and acetate. Photo by: Christine Kenney
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Fig. 2: Projections from the nucleus basalis of Meynert and other cholinergic cell groups in the septum pellucidum to the hippocampus and neocortex. Photo by: Christine Kenney
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Fig. 3: Global impression of change. Clinician's interview-based impression, with caregiver input, of change in global function. Least squares (LS) mean change from baseline scores (and standard error [SE]) for donepezil- and placebo-treated patients through 24 weeks of treatment. LOCF = last observation carried forward. Reprinted, with permission, from Feldman et al. Copyright © 2001 AAN Enterprises, Inc
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Fig. 4: Disability Assessment for Dementia. LS mean change from baseline scores (and SE) for donepezil- and placebo-treated patients through 24 weeks of treatment. Reprinted, with permission, from Feldman et al. Copyright © 2001 AAN Enterprises, Inc
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Fig. 5: Mean change from baseline scores (and SE) on cognitive subscale of Alzheimer's Disease Assessment Scale for galantamine- and placebo-treated patients over time. Reprinted, with permission, from Wilcock et al. Copyright © 2000 BMJ Publishing Group

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